Agarwal, Ram K. and Singh, L. and Sharma, D.K. (2008) Synthesis, spectral and biological properties of copper (Ii) complexes of thiosemicarbazones of schiff bases derived from 4-aminoantipyrine and aromatic aldehydes. Reviews in Inorganic Chemistry, 28 (3). pp. 161-181. ISSN 0193-4929
Full text not available from this repository.Abstract
We have synthesized a novel series of Schiff bases by condensation of 4-aminoantipyrine and various aromatic aldehydes followed by reaction with thiosemicarbazide. These thiosemicarbazones are potential ligands toward transition metal ions. The reaction of copper(II) salts with 4[N-(benzalidene)amino]antipyrinethiosemicarbazone (BAAPTS), 4[N-(4′-methoxybenzalidene) amino] antipyrinethiosemicarbozone (MBAAPTS), 4[N-(4′-dimethylamino benzalidene) amino] antipyrinethiosemicarbazone (DABAAPTS), and 4[N-(cinnamalidene) amino] antipyrinethiosemicarbazone (CAAPTS) resulted in the formation of solid complexes with the general composition CuX2 • (H2O)(L)(X = Cl, Br,NO3,NCS, or CH3COO; L = BAAPTS, MBAAPTS, DABAAPTS, or CAAPTS). These complexes were characterized through elemental analysis, molecular weight, electrical conductance, infrared, electronic spectra, and magnetic susceptibilities at room temperature. Copper(II) complexes with BAAPTS and MBAAPTS were screened for antibacterial and antifungal properties and have exhibited potential activity. Thermal stabilities of two representative complexes were also investigated.
Item Type: | Journal Article |
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Subjects: | Q Science > QD Chemistry |
Divisions: | Faculty of Science, Technology and Environment (FSTE) > School of Biological and Chemical Sciences |
Depositing User: | Ms Neha Harakh |
Date Deposited: | 08 Feb 2008 23:49 |
Last Modified: | 23 Jul 2012 08:48 |
URI: | https://repository.usp.ac.fj/id/eprint/153 |
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